ClinVar Miner

Submissions for variant NM_000834.5(GRIN2B):c.153G>A (p.Lys51=)

dbSNP: rs1057522391
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720264 SCV000527503 likely benign not provided 2021-01-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003766308 SCV004610504 likely benign Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27 2023-12-18 criteria provided, single submitter clinical testing

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